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DO Term : oculocutaneous albinism type IV [DOID:0070098] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the SLC45A2 gene on chromosome 5p13.2.

synonyms:
606574,
OMIM:606574,
OCA4

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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